A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644992



Internal ID21837039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41806692..41806692hg38UCSC Ensembl
chr21:43226518..43226518hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107032
Supporting Variants
Samples
Known GenesPRDM15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644992
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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